{{Rsnum
|rsid=121908292
|Chromosome=13
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CLN5
|position=77000799
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLN5
}}{{omim
|id=608102
|rsnum=121908292
|variant=0005
}}{{ClinVar
|rsid=121908292
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=77574934
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CLN5:1203
|GENE_NAME=CLN5
|GENE_ID=1203
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.77574934G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608102.0005
|CLNSIG=5
|CLNCUI=C1850442
|CLNDBN=Ceroid lipofuscinosis neuronal 5
|Disease=Ceroid lipofuscinosis neuronal 5
|CLNACC=RCV000002677.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1850442:256731:168491:228360
}}